Canonical Allele Identifier: CA1239825385

Gene: OTOF

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.26461702_26461705delinsAGTC , CM000664.2:g.26461702_26461705delinsAGTC	GRCh38
NC_000002.11:g.26684570_26684573delinsAGTC , CM000664.1:g.26684570_26684573delinsAGTC	GRCh37
NC_000002.10:g.26538074_26538077delinsAGTC	NCBI36
NG_009937.1:g.101994_101997delinsGACT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272371.7:c.5524_5527delinsGACT MANE Select	ENSP00000272371.2:p.Asp1842=
ENST00000339598.8:c.3223_3226delinsGACT MANE Plus Clinical	ENSP00000344521.3:p.Asp1075=
ENST00000402415.8:c.3283_3286delinsGACT	ENSP00000383906.4:p.Asp1095=
ENST00000272371.6:c.5524_5527delinsGACT	ENSP00000272371.2:p.Asp1842=
ENST00000338581.10:c.3223_3226delinsGACT	ENSP00000345137.6:p.Asp1075=
ENST00000339598.7:c.3223_3226delinsGACT	ENSP00000344521.3:p.Asp1075=
ENST00000402415.7:c.3454_3457delinsGACT	ENSP00000383906.3:p.Asp1152=
ENST00000403946.7:c.5524_5527delinsGACT	ENSP00000385255.3:p.Asp1842=
NM_001287489.1:c.5524_5527delinsGACT	NP_001274418.1:p.Asp1842=
NM_004802.3:c.3223_3226delinsGACT	NP_004793.2:p.Asp1075=
NM_194248.2:c.5524_5527delinsGACT	NP_919224.1:p.Asp1842=
NM_194322.2:c.3454_3457delinsGACT	NP_919303.1:p.Asp1152=
NM_194323.2:c.3223_3226delinsGACT	NP_919304.1:p.Asp1075=
XM_005264644.2:c.5509_5512delinsGACT	XP_005264701.1:p.Asp1837=
XM_011533185.1:c.5569_5572delinsGACT	XP_011531487.1:p.Asp1857=
XM_017005338.1:c.5464_5467delinsGACT	XP_016860827.1:p.Asp1822=
NM_001287489.2:c.5524_5527delinsGACT	NP_001274418.1:p.Asp1842=
NM_004802.4:c.3223_3226delinsGACT	NP_004793.2:p.Asp1075=
NM_194248.3:c.5524_5527delinsGACT MANE Select	NP_919224.1:p.Asp1842=
NM_194322.3:c.3454_3457delinsGACT	NP_919303.1:p.Asp1152=
NM_194323.3:c.3223_3226delinsGACT MANE Plus Clinical	NP_919304.1:p.Asp1075=